Canonical Allele Identifier: CA245200537

Gene: ATP6V0A2

Linked Data

• dbSNP Id: rs543506966
• gnomAD v3: 12-123744426-G-A
• gnomAD v4: 12-123744426-G-A
• MyVariant Identifiers: chr12:g.124228973G>A (hg19) ; chr12:g.123744426G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123744426G>A , CM000674.2:g.123744426G>A	GRCh38
NC_000012.11:g.124228973G>A , CM000674.1:g.124228973G>A	GRCh37
NC_000012.10:g.122794926G>A	NCBI36
NG_012743.1:g.37109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330342.8:c.1326+89G>A MANE Select	ENSP00000332247.2:n.1326+89G>A
ENST00000540368.6:n.1357+89G>A
ENST00000674794.1:c.1414+89G>A
ENST00000675260.1:n.601+89G>A
ENST00000675344.1:c.*347+89G>A	ENSP00000501953.1:n.*347+89G>A
ENST00000330342.7:c.1326+89G>A	ENSP00000332247.2:n.1326+89G>A
ENST00000504192.2:c.936+89G>A	ENSP00000443441.1:n.936+89G>A
ENST00000536426.1:n.343+89G>A
ENST00000545059.5:n.3962+89G>A
NM_012463.3:c.1326+89G>A	NP_036595.2:n.1326+89G>A
XM_005253563.1:c.1326+89G>A	XP_005253620.1:n.1326+89G>A
XM_006719317.2:c.813+89G>A	XP_006719380.1:n.813+89G>A
XM_006719318.2:c.504+89G>A	XP_006719381.1:n.504+89G>A
XR_429088.1:n.1489+89G>A
XM_024448910.1:c.1326+89G>A	XP_024304678.1:n.1326+89G>A
XM_024448911.1:c.813+89G>A	XP_024304679.1:n.813+89G>A
XM_024448912.1:c.504+89G>A	XP_024304680.1:n.504+89G>A
NM_012463.4:c.1326+89G>A MANE Select	NP_036595.2:n.1326+89G>A